DRIVE PLTCABRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383979526), received between May 27, 2026 and May 27, 2026 — classified as 1 death.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• DeathMay 27, 2026Insufficient Device Problem Information

  DRIVE MEDICAL WAS NOTIFIED OF AN INCIDENT INVOLVING AN ASSIST RAIL BY A PROVIDER, WHO REPORTED THAT A RESIDENT'S NECK WAS WEDGED BETWEEN THE ASSIST RAIL AND THE MATTRESS AND THAT THE RESIDENT PASSED AWAY. THE BED AND THE ASSIST RAIL INVOLVED ARE DRIVE MEDICAL PRODUCTS. THE MATTRESS INVOLVED IS A COMPETITOR'S PRODUCT, NOT A DRIVE MEDICAL PRODUCT. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE MEDICAL WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Physical Entrapment

  MAUDE report 25300553 ↗